The feasibility of using actigraphy to characterize sleep in Rett syndrome
Abstract Background Rett syndrome (RTT) is a neurodevelopmental disorder primarily caused by mutations in the MECP2 gene. Sleep problems are reported by the majority of caregivers of individuals with RTT. Methods The present study aimed to replicate and extend previous work about the feasibility of...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2018-02-01
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Series: | Journal of Neurodevelopmental Disorders |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s11689-018-9227-z |